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IEEE Transactions on Medical Imaging|August 10, 2006
Differentiation of sCJD and vCJD forms by automated analysis of basal ganglia intensity distribution in multisequence MRI of the brain--definition and evaluation of new MRI-based ratiosMarius George Linguraru, Nicholas Ayache, Eric Bardinet, et al.
Brain : a Journal of Neurology|October 23, 2021
An in vivo Caenorhabditis elegans model for therapeutic research in human prion diseasesNicolas Bizat, Valeria Parrales, Sofian Laoues, et al.
Frontiers in Neuroscience|February 7, 2018
Hemoglobin mRNA Changes in the Frontal Cortex of Patients with Neurodegenerative DiseasesSilvia Vanni, Marco Zattoni, Fabio Moda, et al.
Nature Communications|November 4, 2017
Experimental transfusion of variant CJD-infected blood reveals previously uncharacterised prion disorder in mice and macaqueEmmanuel E Comoy, Jacqueline Mikol, Nina Jaffré, et al.
The New England Journal of Medicine|August 8, 2014
Prions in the urine of patients with variant Creutzfeldt-Jakob diseaseFabio Moda, Pierluigi Gambetti, Silvio Notari, et al.
Acta Neuropathologica|December 7, 2017
Neuropathology of iatrogenic Creutzfeldt-Jakob disease and immunoassay of French cadaver-sourced growth hormone batches suggest possible transmission of tauopathy and long incubation periods for the transmission of Abeta pathologyCharles Duyckaerts, Véronique Sazdovitch, Kunie Ando, et al.
Scientific Reports|February 19, 2021
Sensitive protein misfolding cyclic amplification of sporadic Creutzfeldt-Jakob disease prions is strongly seed and substrate dependentMaxime Bélondrade, Simon Nicot, Charly Mayran, et al.
Annals of Neurology|April 1, 2009
Variant Creutzfeldt-Jakob disease in France and the United Kingdom: Evidence for the same agent strainJean-Philippe Brandel, Craig A Heath, Mark W Head, et al.
Plos One|March 26, 2013
Glycoform-selective prion formation in sporadic and familial forms of prion diseaseXiangzhu Xiao, Jue Yuan, Stéphane Haïk, et al.
Science Translational Medicine|December 23, 2016
Detection of prions in the plasma of presymptomatic and symptomatic patients with variant Creutzfeldt-Jakob diseaseDaisy Bougard, Jean-Philippe Brandel, Maxime Bélondrade, et al.
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